NOVO VIVO SUCTION CATHETER VESSEL W/MUCOSE TRAP— 510(k) K880376

Name: FDA 510(k) clearance K880376
Creator: U.S. Food and Drug Administration
Published: 1988-02-16

Substantially Equivalent

Genesis Industries, Inc.

FDA 510(k) clearance K880376 for NOVO VIVO SUCTION CATHETER VESSEL W/MUCOSE TRAP, Substantially Equivalent on 1988-02-16. Applicant: Genesis Industries, Inc.. Device class: 1.

Clearance details

Applicant: Genesis Industries, Inc.
Product code: Code GBS
Device class: Class 1
Regulation: 21 CFR 878.4200
Advisory panel: General, Plastic Surgery
Date received: 1988-01-27
Decision date: 1988-02-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Spring Valley, WI, US

Download summary PDF View on FDA.gov ↗

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K880377 — NOVO VIVO MODEL #17140 AND #171351988-04-04
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